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documentation lms quality assurance regulatory affairs gxp📋 Description
- Lead Document Control compliance and process improvements
- Plan and coordinate document control activities and processes
- Format and issue training documents accurately
- Review Document Change Controls and ensure revision control
- Coordinate periodic reviews with stakeholders
- Perform admin tasks in Veeva QualityDocs and Veeva Training
🎯 Requirements
- Bachelor’s degree or higher
- 5-10 years QA in pharmaceutical industry
- EDMS and LMS experience (Veeva QualityDocs, Veeva Training)
- Strong knowledge of GxP regulations
- Experience resolving Good Documentation Practices issues
- Excellent organizational, interpersonal, and written communication
🎁 Benefits
- Market-leading compensation
- 401(k) with employer match
- 100% employer-paid medical, dental, and vision
- ESPP (Employee Stock Purchase Program)
- Flexible PTO and holidays
- Hybrid work model with flexibility
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